Canonical Allele Identifier: CA344337998
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs1381119367

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159471A>T , CM000663.2:g.204159471A>T GRCh38
NC_000001.10:g.204128599A>T , CM000663.1:g.204128599A>T GRCh37
NC_000001.9:g.202395222A>T NCBI36
NG_012122.1:g.11867T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.617T>A MANE Select ENSP00000272190.8:p.Val206Asp
ENST00000638118.1:c.503T>A ENSP00000490307.1:p.Val168Asp
ENST00000272190.8:c.617T>A ENSP00000272190.8:p.Val206Asp
NM_000537.3:c.617T>A NP_000528.1:p.Val206Asp
NM_000537.4:c.617T>A MANE Select NP_000528.1:p.Val206Asp